ResearcherUniversity of Southern DenmarkNo recent work listed
Ming Tan
Matched on ORCID iD 0000-0003-4935-4152; OpenAlex author ID A5000925263. Sources: OpenAlex.
Their work
- Papers
- 5
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 4
2020: 1 paper · 2021: 3 papers · 2022: 1 paper
Papers 5
- Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. Co-author DOI 10.1111/ahg.12464↗
- Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. Co-author DOI 10.1080/00365521.2021.1937697↗
- Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients. Co-author DOI 10.1111/cge.14038↗
- Heritability of familial pancreatic cancer in a Danish national family cohort Co-author DOI 10.21203/rs.3.rs-141845/v1↗
- Gene Expression Network Analysis of Precursor Lesions in Familial Pancreatic Cancer. Co-author DOI 10.1089/pancan.2020.0007↗
Closest collaborators
The 4 strongest of 4 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Maiken Thyregod Jøergensen · 5 shared papers, 2020–2022 · strength 0.80
- Paper Gene Expression Network Analysis of Precursor Lesions in Familial Pancreatic Cancer. DOI 10.1089/pancan.2020.0007↗
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Ove B. Schaffalitzky de Muckadell · 5 shared papers, 2020–2022 · strength 0.80
- Paper Gene Expression Network Analysis of Precursor Lesions in Familial Pancreatic Cancer. DOI 10.1089/pancan.2020.0007↗
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Michael Bau Mortensen · 4 shared papers, 2021–2022 · strength 0.61
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Paper Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of… DOI 10.1111/cge.14038↗
- Sönke Detlefsen · 4 shared papers, 2021–2022 · strength 0.61
- Paper Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. DOI 10.1111/ahg.12464↗
- Paper Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study. DOI 10.1080/00365521.2021.1937697↗
- Paper Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of… DOI 10.1111/cge.14038↗
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.